ClearanceBrief
510(k) K781634 ยท HCC Device, Biofeedback

VISUALAX

ApplicantFarrall Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 3, 1978
ReceivedSep 22, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781634

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.